Nuclear Medicine Technologist - Theranostics (California)
Telix Pharmaceuticals Limited
August 07, 2026
Remote friendly (United States)
United States
Operations
Job Summary
The Clinical Technical Specialist (CTS) will serve as a key leader in site onboarding, medical education, and radiopharmaceutical optimization, ensuring successful adoption and utilization of Telix products in both commercial and clinical trial settings. The role oversees multiple site activation initiatives, drives cross-functional collaboration, and supports Medical Affairs objectives by shaping research priorities, optimizing imaging protocols, and advancing disease state education.
Key Accountabilities
- Lead and oversee strategic onboarding of new imaging sites, integrating Telix radiopharmaceuticals into commercial and clinical trial workflows.
- Develop and implement best practices for imaging site optimization (protocol standardization, scanner settings, workflow efficiency).
- Oversee field activities aligned with Medical Affairs strategy to support product launches, clinical research, and physician education.
- Identify critical data gaps and real-world evidence opportunities to shape research priorities.
- Lead site engagement with imaging centers, nuclear medicine specialists, and key stakeholders to ensure patient access and product utilization.
- Establish and manage scientific education (training materials and consistent knowledge dissemination).
- Represent Medical Affairs at medical/scientific meetings and synthesize insights to inform strategy.
- Stay current on imaging best practices and emerging technologies.
- Liaise between Medical Affairs and cross-functional teams (Commercial, Marketing, Clinical Operations, Regulatory).
- Manage Medical Affairs projects and initiatives with measurable impact.
Education and Experience / Qualifications
- BS or MS in a scientific discipline (preferred Radiology) or equivalent experience.
- NMTCB or ARRT certification required.
- 5+ years of experience with advanced oncology PET scanning and optimization.
- Radiopharmaceutical experience required (prostate cancer preferred).
- Knowledge of pharmaceutical industry policies.
- Experience interpreting scientific data and market/competitive intelligence.
- Proficient in Microsoft Office Suite.
- Valid driver’s license; travel up to 75%; must live near a major airport and reside in the territory.
Skills / Capabilities
- Excellent verbal and written communication; strong organization, time-management, and interpersonal skills.
- Ability to work independently and in a team; initiative-taking.
- Strong collaboration, ethics, adaptability, resilience, and continuous learning.
The Clinical Technical Specialist (CTS) will serve as a key leader in site onboarding, medical education, and radiopharmaceutical optimization, ensuring successful adoption and utilization of Telix products in both commercial and clinical trial settings. The role oversees multiple site activation initiatives, drives cross-functional collaboration, and supports Medical Affairs objectives by shaping research priorities, optimizing imaging protocols, and advancing disease state education.
Key Accountabilities
- Lead and oversee strategic onboarding of new imaging sites, integrating Telix radiopharmaceuticals into commercial and clinical trial workflows.
- Develop and implement best practices for imaging site optimization (protocol standardization, scanner settings, workflow efficiency).
- Oversee field activities aligned with Medical Affairs strategy to support product launches, clinical research, and physician education.
- Identify critical data gaps and real-world evidence opportunities to shape research priorities.
- Lead site engagement with imaging centers, nuclear medicine specialists, and key stakeholders to ensure patient access and product utilization.
- Establish and manage scientific education (training materials and consistent knowledge dissemination).
- Represent Medical Affairs at medical/scientific meetings and synthesize insights to inform strategy.
- Stay current on imaging best practices and emerging technologies.
- Liaise between Medical Affairs and cross-functional teams (Commercial, Marketing, Clinical Operations, Regulatory).
- Manage Medical Affairs projects and initiatives with measurable impact.
Education and Experience / Qualifications
- BS or MS in a scientific discipline (preferred Radiology) or equivalent experience.
- NMTCB or ARRT certification required.
- 5+ years of experience with advanced oncology PET scanning and optimization.
- Radiopharmaceutical experience required (prostate cancer preferred).
- Knowledge of pharmaceutical industry policies.
- Experience interpreting scientific data and market/competitive intelligence.
- Proficient in Microsoft Office Suite.
- Valid driver’s license; travel up to 75%; must live near a major airport and reside in the territory.
Skills / Capabilities
- Excellent verbal and written communication; strong organization, time-management, and interpersonal skills.
- Ability to work independently and in a team; initiative-taking.
- Strong collaboration, ethics, adaptability, resilience, and continuous learning.